| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs878960 | 0.925 | 0.040 | 15 | 26683789 | intron variant | C/G;T | snv | 2 | |||
| rs4703129 | 1.000 | 0.040 | 5 | 98553032 | intergenic variant | C/A | snv | 0.33 | 1 |